ClearanceBrief
510(k) K973138 ยท BZG Spirometer, Diagnostic

SPIROCARD

ApplicantQrs Diagnostic, LLC, Plymouth MN, US
DecisionSubstantially Equivalent, Oct 28, 1998
ReceivedAug 21, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973138

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.